PROK2, prokineticin 2, 60675

N. diseases: 151; N. variants: 11
Disease: Kallmann Syndrome ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs587777863
rs587777863
Entrez Id: 60675;105377156
Gene Symbol: PROK2;LOC105377156
PROK2;LOC105377156
CUI: C0162809
Disease:
Kallmann Syndrome 		0.010 GeneticVariation BEFREE Among them, six had KS, four nIHH, and one KS proband carried both a PROKR2 (p.V115M) and PROK2 (p.A24P) mutation. 18559922 2008